de la cruz tincture of iodine
Generic: iodine and sodium iodide and alcohol
Labeler: dlc laboratories, inc.Drug Facts
Product Profile
Brand Name
de la cruz tincture of iodine
Generic Name
iodine and sodium iodide and alcohol
Labeler
dlc laboratories, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 470 mg/mL, iodine 20 mg/mL, sodium iodide 20.4 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
24286-1528
Product ID
24286-1528_0c940d4f-cca2-7175-e063-6394a90af568
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
1979-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
242861528
Hyphenated Format
24286-1528
Supplemental Identifiers
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
de la cruz tincture of iodine (source: ndc)
Generic Name
iodine and sodium iodide and alcohol (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 470 mg/mL
- 20 mg/mL
- 20.4 mg/mL
Packaging
- 30 mL in 1 BOTTLE (24286-1528-7)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0c940d4f-cca2-7175-e063-6394a90af568", "openfda": {"upc": ["0324286153015"], "unii": ["3K9958V90M", "9679TC07X4", "F5WR8N145C"], "spl_set_id": ["5d8f60a9-6d1c-0b0f-e053-2991aa0a8a9b"], "manufacturer_name": ["DLC Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (24286-1528-7)", "package_ndc": "24286-1528-7", "marketing_start_date": "20171027"}], "brand_name": "De La Cruz Tincture of Iodine", "product_id": "24286-1528_0c940d4f-cca2-7175-e063-6394a90af568", "dosage_form": "LIQUID", "product_ndc": "24286-1528", "generic_name": "Iodine and Sodium Iodide and Alcohol", "labeler_name": "DLC Laboratories, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "De La Cruz Tincture of Iodine", "active_ingredients": [{"name": "ALCOHOL", "strength": "470 mg/mL"}, {"name": "IODINE", "strength": "20 mg/mL"}, {"name": "SODIUM IODIDE", "strength": "20.4 mg/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19790101", "listing_expiration_date": "20261231"}